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ECHO-COPD: Impact of a Pharmacist-Led Health Belief Model-Based Educational Intervention Among COPD Patients (ECHO-COPD)

2026년 9월 7일 업데이트: Rabia Hussain

Impact of a Pharmacist-Led Health Belief Model-Based Educational Intervention on Medication Adherence, Quality of Life, and Direct Cost Among COPD Patients at Buraidah Central Hospital in Al-Qassim Region, Saudi Arabia: A Quasi-Experimental Design

Chronic obstructive pulmonary disease (COPD) is a chronic respiratory disease associated with substantial morbidity and mortality, impaired quality of life, and healthcare costs. Medication adherence and appropriate self-management are important components of COPD management; however, patients' health beliefs and perceptions may influence their adherence to treatment and engagement in recommended health behaviours. This study aims to evaluate the impact of a pharmacist-led educational intervention based on the Health Belief Model (HBM) on medication adherence, quality of life, and direct healthcare costs among patients with COPD receiving care at Buraidah Central Hospital (BCH) in Al-Qassim Region, Saudi Arabia.

A quantitative, quasi-experimental pretest-posttest control-group design will be used. Eligible COPD patients will be non-randomly assigned to either an intervention group or a control group. The intervention group will receive structured, pharmacist-led HBM-based educational sessions in addition to routine care. In contrast, the control group will continue to receive standard care without additional educational input. Baseline assessments will include medication adherence using the 8-item Morisky Medication Adherence Scale (MMAS-8); quality of life and health status using the COPD Assessment Test (CAT); health beliefs using a structured HBM questionnaire; and direct medical costs obtained from the hospital clinical cost centre. The educational intervention will be delivered over six months, followed by post-intervention assessment using the same outcome measures.

연구 개요

상세 설명

The HBM will guide the content and delivery of the pharmacist-led educational intervention. The intervention will address the six core constructs of the HBM:

  1. Perceived susceptibility
  2. Perceived severity
  3. Perceived benefits
  4. Perceived barriers
  5. Cues to action
  6. Self-efficacy The purpose of applying the HBM is to influence patients' understanding of COPD and promote positive behavioural changes, particularly improvements in medication adherence. The study will then examine the relationship between these improvements and quality of life, healthcare utilisation, and direct healthcare costs.

The intervention will consist of structured face-to-face educational sessions conducted in the designated counselling room of the Pulmonary Department at BCH. Sessions will incorporate printed educational materials, lectures, counselling, practical demonstrations, motivational support, problem-solving strategies, and reinforcement of behavioural changes.

The educational programme will cover aspects of COPD management, medication adherence and appropriate medication use, COPD risk factors and complications, nutrition and preventive care, smoking cessation, barriers to recommended behaviours, cues to action, and strategies to improve patients' confidence in managing COPD.

Participants in the intervention and control groups will undergo pre-intervention assessments. Participants in the intervention group will subsequently receive the structured educational programme, while the control group will continue to receive standard care without additional educational input. Post-intervention assessments will use the same measurement instruments to allow within-group and between-group comparisons.

연구 유형

중재적

등록 (추정된)

140

단계

  • 해당 없음

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

연구 연락처 백업

연구 장소

    • Al-Qassim Region
      • Buraidah, Al-Qassim Region, 사우디 아라비아, 52391
        • Bander S Alshammeri
        • 연락하다:

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

  • 성인
  • 고령자

건강한 자원 봉사자를 받아들입니다

아니

설명

Inclusion Criteria:

Participants must:

  1. Be adults aged 18-65 years.
  2. Be diagnosed with COPD stages I-III according to GOLD guidelines.
  3. Have visited or been admitted for a COPD exacerbation and be receiving care at BCH in Al-Qassim Region, Saudi Arabia.
  4. Be Arabic-speaking and capable of understanding study instructions.
  5. Be willing and able to provide written informed consent.

Exclusion Criteria:

Participants will be excluded if they:

  1. Are diagnosed with COPD stage IV.
  2. Have another significant pulmonary disease, including:

    • Asthma
    • Bronchiectasis
    • Pneumonia
    • Cystic fibrosis
  3. Have a serious systemic illness, severe comorbidity, or central organ dysfunction, including:

    • Hepatic dysfunction
    • Renal dysfunction
    • Psychiatric impairment
    • Sensory impairment
  4. Are immunocompromised or receiving immunosuppressive treatment.
  5. Have psychological, sensory, or cognitive impairment that prevents meaningful participation in the study.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 건강 서비스 연구
  • 할당: 무작위화되지 않음
  • 중재 모델: 병렬 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: HBM-Based Educational Intervention

Participants in the intervention group will receive routine care together with structured pharmacist-led educational sessions based on the HBM.

The educational intervention will be conducted face-to-face during scheduled outpatient appointments in the designated counselling room of the Pulmonary Department.

The programme will be delivered from study months 4 to 9.

Educational sessions will include:

  • Printed educational materials
  • Lectures
  • Individual counselling
  • Practical demonstrations
  • Personalised feedback
  • Problem-solving strategies
  • Motivational support
  • Interactive activities
  • Peer group discussions
  • Reinforcement of behavioural changes The six HBM constructs will guide the educational content.

Participants in the intervention group will receive routine care together with structured pharmacist-led educational sessions based on the HBM.

The educational intervention will be conducted face-to-face during scheduled outpatient appointments in the designated counselling room of the Pulmonary Department.

The programme will be delivered from study months 4 to 9.

Educational sessions will include:

  • Printed educational materials
  • Lectures
  • Individual counselling
  • Practical demonstrations
  • Personalised feedback
  • Problem-solving strategies
  • Motivational support
  • Interactive activities
  • Peer group discussions
  • Reinforcement of behavioural changes The six HBM constructs will guide the educational content.
간섭 없음: Standard Care

Participants in the control group will continue to receive routine/standard care provided by BCH.

They will not receive the additional structured pharmacist-led HBM-based educational intervention.

Both intervention and control participants will undergo the same baseline and post-intervention assessments.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Medication Adherence
기간: Baseline and 6 months after initiation of the educational intervention.
Change in medication adherence Measurement Tool 8-item Morisky Medication Adherence Scale (MMAS-8), prevalidated Arabic version Medication adherence will be assessed using MMAS-8 at baseline and following completion of the intervention.
Baseline and 6 months after initiation of the educational intervention.

2차 결과 측정

결과 측정
측정값 설명
기간
Quality of Life and Health Status
기간: Baseline and 6 months after initiation of the educational intervention.
Change in quality of life/health status Measurement Tool COPD Assessment Test (CAT), prevalidated Arabic version The CAT will be administered to participants in both groups at baseline and after completion of the intervention.
Baseline and 6 months after initiation of the educational intervention.
Direct Healthcare Costs
기간: Direct medical costs assessed during the pre-intervention baseline period and during the post-intervention follow-up period after completion of the six-month intervention.

Change in direct medical costs associated with COPD Direct medical cost data will be obtained from the clinical cost centre of BCH.

The costing analysis will include direct COPD-related healthcare resources such as:

  • Medications
  • Laboratory tests
  • Chest X-rays
  • Oxygen therapy Other direct medical resources documented within the approved data-collection instrument will be included as applicable.

Important Costing Specification The cost of delivering the educational intervention will not be included in the costing analysis.

The economic component of this study focuses on the direct cost of illness associated with COPD rather than the cost of implementing the educational intervention.

Direct medical costs assessed during the pre-intervention baseline period and during the post-intervention follow-up period after completion of the six-month intervention.

기타 결과 측정

결과 측정
측정값 설명
기간
HBM Constructs
기간: Baseline and 6 months after initiation of the educational intervention.

Changes in patients' health beliefs will be assessed using a structured, prevalidated Arabic HBM questionnaire.

The questionnaire assesses:

  • Perceived susceptibility
  • Perceived severity
  • Perceived benefits
  • Perceived barriers
  • Cues to action
  • Self-efficacy
Baseline and 6 months after initiation of the educational intervention.

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (추정된)

2026년 9월 1일

기본 완료 (추정된)

2027년 8월 30일

연구 완료 (추정된)

2027년 8월 31일

연구 등록 날짜

최초 제출

2026년 9월 7일

QC 기준을 충족하는 최초 제출

2026년 9월 7일

처음 게시됨 (실제)

2026년 9월 11일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 9월 11일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 9월 7일

마지막으로 확인됨

2026년 9월 1일

추가 정보

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아니요

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